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659789 Sigma-Aldrich

Potassium 3-carboxyphenyltrifluoroborate

97%

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Properties

Related Categories Aryl Trifluoroborate Salts, Boronic Acids and Derivatives, Chemical Synthesis, Organometallic Reagents, Trifluoroborate Salts More...
assay   97%
mp   >300 °C
SMILES string   [K+].OC(=O)c1cccc(c1)[B-](F)(F)F
InChI   1S/C7H5BF3O2.K/c9-8(10,11)6-3-1-2-5(4-6)7(12)13;/h1-4H,(H,12,13);/q-1;+1
InChI key   LKEMWADDENRLDB-UHFFFAOYSA-N

Description

Application

Organotrifluoroborate involved in cross-coupling reactions with halopurines

Organotrifluoroborates as versatile and stable boronic acid surrogates.

Packaging

1, 5 g in glass bottle

Safety & Documentation

Safety Information

Symbol 
GHS07  GHS07
Signal word 
Warning
Hazard statements 
Precautionary statements 
Personal Protective Equipment 
RIDADR 
NONH for all modes of transport
WGK Germany 
3
Protocols & Articles

Related Content

Organotrifluoroborates in Chemical Synthesis

Potent Boronic Acid Surrogates In the vast array of catalytic carbon-carbon bond forming reactions, the Suzuki-Miyaura protocol has proven to be a particularly attractive method.  The organoborane nu...
Keywords: Addition reactions, Catalysis, Coupling reactions, Cross couplings, Halogenations, Suzuki-Miyaura coupling

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